ProPharma Group is an industry leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in Australia, Canada, Germany, Japan, the Netherlands, Sweden, United Kingdom, and the United States, ProPharma Group’s fully integrated service offerings will provide clients with a comprehensive suite of global support services that are required to be competitive in today’s dynamic markets. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes.
Writing technical responses such as letters or frequently asked questions (FAQs) to be used to answer enquiries received by Medical Information. This may involve updating existing responses or writing new standard responses. Essential Functions Include: 1. Medical Information service delivery 2. Quality Assurance Extensive training, supervision, mentoring and advice will be provided to support the Associate Medical Information Writer in the conduct of the designated responsibilities listed below: 1. A human life sciences degree. 2. Excellent written communication skills. 3. Computer literacy. 4. Sound planning, prioritising and organisational skills. 5. Excellent accuracy and attention to detail. 6. Able to work within a team in an open and professional manner. All candidates must be legally eligible to work in the United Kingdom. ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***Job Description
• Quality checking own work and that of others within the team under guidance to ensure standards are met and maintained.
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